In life sciences manufacturing, inspections by the FDA, state regulators or other agencies are part of the job. But too often ...
Zydus Lifesciences Limited has informed stock exchanges that the United States Food and Drug Administration (USFDA) has ...
Unichem Laboratories Limited has informed that the United States Food and Drug Administration (USFDA) has concluded an inspection of the company's Kolhapur active ...
Unichem Laboratories said the United States Food and Drug Administration (USFDA) inspected its Kolhapur API facility from 27 January to 2 February 2026.
With a potential US government shutdown looming, Megha Sinha, Kamet Consulting, says to treat FDA disruptions as predictable risks by protecting milestones and early readiness.
The new Quality Management System Regulation (QMSR) that became effective on February 2, 2026, includes significant changes ...
Many organizations are operating with constrained resources while trying to expand, launch new therapies, or scale ...
The US Food and Drug Administration (FDA) and the European Medicines Agency (EMA) just issued a joint statement outlining 10 “Guiding Principles” ...
Zydus Lifesciences share price rose in the early trade on January 27 despite the company received three observations from the ...
Annature Launches 21 CFR Part 11 Compliant Digital Signatures to Support FDA-Regulated Organisations
BRISBANE, AU / ACCESS Newswire / February 5, 2026 / Annature, Australia's leading eSignature and Identity verification ...
Unichem Laboratories said the USFDA inspected its Kolhapur API facility, closing the audit with five procedural observations. Shares ended higher even as Q3 profit fell 20.5% year-on-year.
The integrated solution delivers a shift-left approach to cybersecurity, enabling executive teams to proactively embed security, quality, and compliance from early development to post-market. When ...
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